PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis
Paolo Emidio Macchia(University of Naples Federico II), Roberto Di Lauro(Stazione Zoologica Anton Dohrn), Paola Lapi(Stazione Zoologica Anton Dohrn), Caterina Missero(Ceinge Biotecnologie Avanzate (Italy)), Gianfranco Fenzi(University of Naples Federico II), Maria Teresa Pirro(Casa Sollievo della Sofferenza), Vittorio Tassi(Casa Sollievo della Sofferenza), Annette Grüters(Humboldt-Universität zu Berlin), Mariangiola Baserga(University of Reggio Calabria), Meinrad Busslinger(Research Institute of Molecular Pathology), Luca Chiovato, Abdallah Souabni(Research Institute of Molecular Pathology), Heiko Krude(Humboldt-Universität zu Berlin), Aldo Pinchera
Cited by 502
Related Papers
Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans
|Nature Genetics|1998|1.7k
Proopiomelanocortin Deficiency Treated with a Melanocortin-4 Receptor Agonist
|New England Journal of Medicine|2016|469
Childhood Obesity
|The Journal of Clinical Endocrinology & Metabolism|2005|416
Surgery or Surveillance for Mild Asymptomatic Primary Hyperparathyroidism: A Prospective, Randomized Clinical Trial
|The Journal of Clinical Endocrinology & Metabolism|2007|406
Consensus statement : Childhood obesity
|Unknown|2005|392